A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998381



Internal ID6734317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4847681..4849021hg38UCSC Ensembl
chr16:4897682..4899022hg19UCSC Ensembl
chr16:4837683..4839023hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381341
hg191341
hg181341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3566478
SamplesHuRef
Known GenesUBN1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998381
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer